Principal Clinical Job at Oracle Careers | Medical Candidates Apply
Looking for a senior-level clinical job in healthcare technology? This Principal Clinical Consultant opportunity at Oracle Corporation offers experienced clinicians the chance to drive innovation in medical device software, regulatory strategy, and AI-powered healthcare solutions. Explore one of the most impactful Oracle jobs available in India for professionals with strong expertise in clinical risk, usability engineering, and regulatory compliance.
Job Details:
- Job Title: Principal Clinical Consultant
- Location: India
- Job Identification: 312737
- Job Category: Consulting
- Role: Individual Contributor
- Job Type: Regular Employee
- Language Requirement: English
- Experience Required: 6 to 10+ years
About the Company
Oracle Corporation brings together data, infrastructure, applications, and expertise to power everything from industry innovations to life-saving care. With AI embedded across products and services, Oracle helps customers transform healthcare and other industries through advanced cloud and digital solutions. Oracle careers offer opportunities to work on cutting-edge AI-driven technologies impacting billions of lives worldwide.
Job Description
This senior-level clinical job focuses on providing deep domain expertise in clinical workflows, usability engineering, and patient safety within healthcare technology and medical device environments. The role supports regulatory alignment, clinical risk analysis, and cross-functional collaboration across product management, engineering, and compliance teams. This MD job opportunity is ideal for experienced clinicians seeking to transition into high-impact Oracle careers in digital health and medical device innovation.
Qualifications
- Licensed clinician (MD, PA, or equivalent) with 10+ years of clinical experience.
- Minimum 10+ years’ experience in product management, clinical informatics, or usability/human factors engineering within healthcare technology or medical devices.
- Knowledge of ISO 14971, IEC 62366, EU MDR/IVDR, and FDA guidance related to medical device software (SaMD).
- Strong understanding of clinical risk, safety analysis, and usability validation methodologies.
- Proven ability to translate complex clinical workflows into clear design and engineering requirements.
- Excellent cross-functional communication and documentation skills.
Preferred:
- Experience supporting regulatory submissions or audits (EU MDR, FDA 510(k), etc.).
- Experience working with AI-driven medical device applications or software as a medical device (SaMD).
- Familiarity with Oracle Health/Cerner Millennium or similar EHR platforms.
- Advanced degree in healthcare informatics, biomedical engineering, or related field.
Key Responsibilities:
- Conduct and contribute to clinical risk analyses (per ISO 14971).
- Collaborate on Failure Mode and Effects Analyses (FMEAs), hazard analyses, and usability studies for clinical safety.
- Partner with engineering teams to identify and mitigate clinical risks across design and implementation.
- Serve as a Clinical and Product-Focused Specialist, providing deep domain expertise in clinical workflows, usability, and patient safety.
- Provide clinical context for Clinical Evaluation Reports (CERs), including alignment with EU MDR and FDA regulatory requirements.
- Oversee usability engineering (IEC 62366), ensuring requirements map to user needs and validation meets usability and human factors standards.
- Lead change management oversight across device-relevant business areas (internal and external), ensuring documentation, communication, and validation of changes.
- Act as a bridge between Product Management, Clinical Safety, and Health Compliance Organizations (HCOs).
- Facilitate regulatory awareness and readiness across the broader product organization.
- Partner closely with Medical Device Tiger Teams and transition into broader next-generation device initiatives.
